141-20-8 Usage
Description
Diethylene Glycol Monolaurate, also known as a self-dispersing surface active agent, is a non-ionic surfactant with potent detergent properties. It is a liquid chemical compound that serves as an emulsifier and auxiliary agent, particularly well-suited for use in mineral oil systems.
Uses
Used in Textile Industry:
Diethylene Glycol Monolaurate is used as a dispersing agent and emulsifier for improving the efficiency of dyeing and finishing processes, enhancing the quality of textile products, and reducing environmental impact.
Used in Cosmetics Industry:
Diethylene Glycol Monolaurate is used as an emulsifier for formulating creams, lotions, and other cosmetic products, providing stable emulsions and improving the texture and feel of the final products.
Used in Coatings Industry:
Diethylene Glycol Monolaurate is used as a plasticizer and emulsifier in the coatings industry, contributing to the improved flexibility, durability, and water resistance of the coatings.
Used as a Detergent:
Diethylene Glycol Monolaurate is used as a potent nonionic detergent in various cleaning products, providing effective cleaning power and reducing the environmental impact of the detergents.
Check Digit Verification of cas no
The CAS Registry Mumber 141-20-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,4 and 1 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 141-20:
(5*1)+(4*4)+(3*1)+(2*2)+(1*0)=28
28 % 10 = 8
So 141-20-8 is a valid CAS Registry Number.
InChI:InChI=1/C16H32O4/c1-2-3-4-5-6-7-8-9-10-11-16(18)20-15-14-19-13-12-17/h17H,2-15H2,1H3
141-20-8Relevant articles and documents
PRECIPITATION POLYMERIZATION IN THE PRESENCE OF GLYCERIN MONOSTEARATE
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, (2011/06/28)
A process for preparing a copolymer composition A) by free-radical copolymerization of a monomer composition comprising: a) acrylic acid, b) optionally at least one compound, different from a), having a free-radically polymerizable, α,β-ethylenically unsaturated double bond and at least one anionogenic and/or anionic group per molecule, c) at least one free-radically polymerizable crosslinking compound which comprises at least two α,β-ethylenically unsaturated double bonds per molecule. The process is performed by precipitation polymerization in the presence of an auxiliary composition H) comprising H1) glycerol monostearate, and H2) at least one compound with an HLB value in the range from 4 to 10, selected from water-insoluble natural waxes, nonionic emulsifiers and mixtures thereof.
